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Application of a risk-management framework for integration of stromal tumor-infiltrating lymphocytes in clinical trials

  • International Immuno-Oncology Biomarker Working Group
    ,
  • Jan Hudeček(Author)
    ,
  • Leonie Voorwerk(Author)
    ,
  • Maartje van Seijen(Author)
    ,
  • Iris Nederlof(Author)
    ,
  • Michiel de Maaker(Author)
*Corresponding author for this work
  • The Netherlands Cancer Institute
    ,
  • Ghent University Hospital
    ,
  • New York University Medical School
    ,
  • Weill Cornell Medicine
    ,
  • Istituto di Ricovero e Cura a Carattere Scientifico and International Breast Cancer Study Group
    ,
  • Università degli Studi di Milano
Research Output:
Contribution to journal
Review article
Peer-review

Open access

Publication Information

Output type

Research Output:
Contribution to journal
Review article
Peer-review

Original language

English

Article number

15

Journal (Volume, Issue Number)

npj Breast Cancer (Volume 6, Issue 1)

Publication milestones

  • Published - 01/12/2020

Publication status

Published - 01/12/2020

Publication IDs

  • Scopus: 85083420171

Abstract

Stromal tumor-infiltrating lymphocytes (sTILs) are a potential predictive biomarker for immunotherapy response in metastatic triple-negative breast cancer (TNBC). To incorporate sTILs into clinical trials and diagnostics, reliable assessment is essential. In this review, we propose a new concept, namely the implementation of a risk-management framework that enables the use of sTILs as a stratification factor in clinical trials. We present the design of a biomarker risk-mitigation workflow that can be applied to any biomarker incorporation in clinical trials. We demonstrate the implementation of this concept using sTILs as an integral biomarker in a single-center phase II immunotherapy trial for metastatic TNBC (TONIC trial, NCT02499367), using this workflow to mitigate risks of suboptimal inclusion of sTILs in this specific trial. In this review, we demonstrate that a web-based scoring platform can mitigate potential risk factors when including sTILs in clinical trials, and we argue that this framework can be applied for any future biomarker-driven clinical trial setting.

Funding Details

The Department of Pathology of the Netherlands Cancer Institute is thanked for the support of this study and ensuring the rapid turnaround times. The Breast Cancer Research Foundation and Bristol-Myers-Squibb (BMS) are thanked for financial support. We also thank the BMS-International Immuno-Oncology Network (BMS/II-ON) and the Dutch Cancer Society (NKI2015-7710) for funding the clinical trial costs and this feasibility study (NKI2016-10510). S.L., R.S., and M.K. are supported by a grant from the Breast Cancer Research Foundation (BCRF, NY, US). The following is a list of current members of the International Immuno-Oncology Working Group (TILs Working Group). A member is defined as a person willing to be involved, informed and be part of the activities of the TILs Working Group. The authors alone are responsible for the views expressed in the work of the TIL Working Group and they do not necessarily represent the decisions, policy, or views of their employer.
FundersFunding numbers
BMS-International Immuno-Oncology Network
-
II-ON
-
BCRF
-
BMS
-
DCS
NKI2015-7710, NKI2016-10510

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